戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7709作成日:2026年10月23日

Triethylamine → 2-(3-{[Tert-butyl-(dimethyl)silyl]oxy}-4-methylphenyl)-1,3-benzoxazole

https://huagongshe.com/ja/reaction/7709

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl AcetateHCID 8857—
反応物tert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
反応物5-(1,3-Benzoxazol-2-yl)-2-methylphenolHCID 21991000—
溶媒DichloromethaneHCID 6344—
生成物2-(3-{[Tert-butyl-(dimethyl)silyl]oxy}-4-methylphenyl)-1,3-benzoxazoleHCID 69584544—

反応手順

A solution of 5-(1,3-benzoxazol-2-yl)-2-methylphenol (0.8 g, 3.5 mmol) and triethylamine (0.6 mL, 4.3 mmol) in CH2Cl2 (20 mL) was cooled to 0° C. and TBDMS-OTf (900 mL, 3.9 mmol) was added. The reaction was slowly warmed to rt and EtOAc (200 mL) was added. The mixture was washed with H2O (3×50 mL), dried (MgSO4), filtered, and concentrated in vacuo to afford 2-(3-{[tert-butyl-(dimethyl)silyl]oxy}-4-methylphenyl)-1,3-benzoxazole as light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087601B2
出典データセットuspto-grants-2006_08
ORD IDord-9672a9bf59e345cd9f19654b6ed0dbbb
出典メモuspto-grants-2006_08